Canonical Allele Identifier: CA326720577

Gene: MSL3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.11763920G>A , CM000685.2:g.11763920G>A	GRCh38
NC_000023.10:g.11782039G>A , CM000685.1:g.11782039G>A	GRCh37
NC_000023.9:g.11691960G>A	NCBI36
NG_012564.1:g.10762G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312196.10:c.890G>A MANE Select	ENSP00000312244.4:p.Ser297Asn
ENST00000337339.7:c.890G>A	ENSP00000338078.2:p.Ser297Asn
ENST00000380691.3:c.251G>A	ENSP00000370067.2:p.Ser84Asn
ENST00000380693.8:c.392G>A	ENSP00000370069.4:p.Ser131Asn
ENST00000398527.7:c.854G>A	ENSP00000381538.2:p.Ser285Asn
ENST00000473380.2:n.1179G>A
ENST00000482871.6:c.392G>A	ENSP00000498064.1:p.Ser131Asn
ENST00000647701.1:n.904G>A
ENST00000647857.1:c.890G>A	ENSP00000497753.1:p.Ser297Asn
ENST00000647869.1:c.890G>A	ENSP00000497615.1:p.Ser297Asn
ENST00000647985.1:n.1645G>A
ENST00000648013.1:c.392G>A	ENSP00000497518.1:p.Ser131Asn
ENST00000648207.1:n.936G>A
ENST00000648614.1:c.392G>A	ENSP00000497799.1:p.Ser131Asn
ENST00000648889.1:n.2013G>A
ENST00000648918.1:n.2005G>A
ENST00000649078.1:c.392G>A	ENSP00000498017.1:p.Ser131Asn
ENST00000649130.1:c.790G>A
ENST00000649271.1:c.392G>A	ENSP00000496967.1:p.Ser131Asn
ENST00000649308.1:n.958G>A
ENST00000649602.1:c.392G>A	ENSP00000498168.1:p.Ser131Asn
ENST00000649649.1:c.443G>A	ENSP00000497137.1:p.Ser148Asn
ENST00000649684.1:n.947G>A
ENST00000649685.1:c.443G>A	ENSP00000497496.1:p.Ser148Asn
ENST00000649785.1:c.392G>A	ENSP00000496803.1:p.Ser131Asn
ENST00000649797.1:c.392G>A	ENSP00000498062.1:p.Ser131Asn
ENST00000649851.1:c.392G>A	ENSP00000497132.1:p.Ser131Asn
ENST00000649988.1:n.2037G>A
ENST00000650050.1:n.425G>A
ENST00000650215.1:c.443G>A	ENSP00000496944.1:p.Ser148Asn
ENST00000650370.1:c.*696G>A	ENSP00000498088.1:n.*696G>A
ENST00000650628.1:c.392G>A	ENSP00000496838.1:p.Ser131Asn
ENST00000312196.8:c.890G>A	ENSP00000312244.4:p.Ser297Asn
ENST00000337339.6:c.890G>A	ENSP00000338078.2:p.Ser297Asn
ENST00000361672.6:c.443G>A	ENSP00000354562.2:p.Ser148Asn
ENST00000380691.2:c.251G>A	ENSP00000370067.2:p.Ser84Asn
ENST00000380692.6:c.392G>A	ENSP00000370068.2:p.Ser131Asn
ENST00000380693.7:c.392G>A	ENSP00000370069.3:p.Ser131Asn
ENST00000398527.6:c.854G>A	ENSP00000381538.2:p.Ser285Asn
ENST00000468149.5:c.*423G>A	ENSP00000418673.1:n.*423G>A
ENST00000494268.1:n.793G>A
NM_001193270.2:c.854G>A	NP_001180199.1:p.Ser285Asn
NM_001282174.1:c.443G>A	NP_001269103.1:p.Ser148Asn
NM_006800.3:c.392G>A	NP_006791.2:p.Ser131Asn
NM_078628.1:c.890G>A	NP_523352.1:p.Ser297Asn
NM_078629.3:c.890G>A	NP_523353.2:p.Ser297Asn
XM_005274440.2:c.392G>A	XP_005274497.1:p.Ser131Asn
XM_006724461.1:c.443G>A	XP_006724524.1:p.Ser148Asn
XM_011545442.1:c.890G>A	XP_011543744.1:p.Ser297Asn
XM_011545443.1:c.890G>A	XP_011543745.1:p.Ser297Asn
XM_011545444.1:c.890G>A	XP_011543746.1:p.Ser297Asn
XM_005274440.3:c.392G>A	XP_005274497.1:p.Ser131Asn
XM_011545442.3:c.890G>A	XP_011543744.1:p.Ser297Asn
XR_001755649.2:n.942G>A
NM_006800.4:c.392G>A	NP_006791.2:p.Ser131Asn
NM_078629.4:c.890G>A MANE Select	NP_523353.2:p.Ser297Asn
NM_078628.2:c.890G>A	NP_523352.1:p.Ser297Asn